# FDA recall D-266-2013

> **The Menz Club, LLC** · Class I · drug recall initiated 2012-03-10.

## Product

Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS

## Reason for recall

Marketed without an Approved NDA/ANDA; product found to contain sulfoaildenafil, an analogue of sildenafil, the active ingredient in a FDA approved product used for erectile dysfunction, making it an unapproved new drug

## Distribution

Utah

## Key facts

- **Recall number:** D-266-2013
- **Recalling firm:** The Menz Club, LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2012-03-10
- **Report date:** 2013-04-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ridgeland, MS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-266-2013

## Citation

> AI Analytics. FDA recall D-266-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-266-2013. Source: US FDA. Licensed CC0.

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